510(k) Report

510(k) · Cleared

Cleared

IL1430 Bgelectrolyte Analyzer

K935069510(k) TraditionalCleared Mar 28, 1994154-day reviewClass II21 CFR 862.1120

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Instrumentation Laboratory CO · CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

Cleared on Mar 28, 1994 after a 154-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 21 later devices descend from it.

Decided
Mar 28, 1994
Review
154 days
Class
Class II
Product code
CHL
Recalls
None
Predicates
0

21 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared2006: 1 descendant cleared1997: 1 descendant cleared1999: 1 descendant cleared2011: 1 descendant cleared2012: 1 descendant cleared2010: 1 descendant cleared2002: 1 descendant cleared2005: 1 descendant cleared2016: 5 descendants cleared2014: 1 descendant cleared2017: 1 descendant cleared2019: 2 descendants cleared2021: 1 descendant cleared2023: 2 descendants cleared1990200020102020
  1. This deviceK935069 IL1430 Bgelectrolyte AnalyzerInstrumentation Laboratory CO · 1994
  2. Descendant · cites it directly · 20 of its ownK963800 IL SynthesisInstrumentation Laboratory CO · 1996
  3. Descendant · 2 generations on · 18 of its ownK992834 Gem Premier 3000Instrumentation Laboratory CO · 1999 · Recalled
  4. Descendant · 3 generations on · 17 of its ownK022158 Iqm (Intelligent Quality Management) on the Gem Premier 3000, CVP…Instrumentation Laboratory CO · 2002
  5. Descendant · 4 generations on · 16 of its ownK052121 Gem Premier 3000Instrumentation Laboratory CO · 2005 · Recalled
  6. Descendant · 2 generations on · 14 of its ownK061974 Gem Premier 4000 with Iqm, Model 4000; Gem CVP 1 and 2 with CO-OX…Instrumentation Laboratory CO · 2006 · Recalled

Showing 5 of 21 descendants. See all descendants

Descendants cleared per year

1996: 11997: 11999: 12002: 12005: 12006: 12010: 12011: 12012: 12014: 12016: 52017: 12019: 22021: 12023: 2
1996high 5 (2016) · low 0 (1998)2026

Most influential descendants

Showing 5 of 21 · See all
  • K963800IL SynthesisInstrumentation Laboratory CO · 1996 · cites it directly20descendants
  • K992834Gem Premier 3000Instrumentation Laboratory CO · 1999 · 2 generations on18descendants
  • K022158Iqm (Intelligent Quality Management) on the Gem Premier 3000, CVP (Calibration…Instrumentation Laboratory CO · 2002 · 3 generations on17descendants
  • K052121Gem Premier 3000Instrumentation Laboratory CO · 2005 · 4 generations on16descendants
  • K061974Gem Premier 4000 with Iqm, Model 4000; Gem CVP 1 and 2 with CO-OX; Gem CVP 3 and 4…Instrumentation Laboratory CO · 2006 · 2 generations on14descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K935069IL1430 Bgelectrolyte AnalyzerInstrumentation Laboratory CO1994—
+1K963800IL SynthesisInstrumentation Laboratory CO1996—
+2K992834Gem Premier 3000Instrumentation Laboratory CO19995
+3K022158Iqm (Intelligent Quality Management) on the Gem Premier 3000, CVP (Calibration…Instrumentation Laboratory CO2002—
+4K052121Gem Premier 3000Instrumentation Laboratory CO20052
+2K061974Gem Premier 4000 with Iqm, Model 4000; Gem CVP 1 and 2 with CO-OX; Gem CVP 3…Instrumentation Laboratory CO20064

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
199910
200210
200510
200610
201010
201110
201210
201410
201650
201710
201920
202110
202320
FIG. 1 — Lineage of K935069, 1994–2023Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in CHL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new CHL device

  1. #1 K252207 ABL90 FLEX PLUS System, safeCLINITUBESscore 14.2 · 11 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (21)

See all 21

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K963800IL SynthesisInstrumentation Laboratory CO199620

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K963800 (Instrumentation Laboratory CO, 1996) has gone furthest, with 20 descendants of its own.

How does its category compare?

All CHL devices

CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CHL

1in 2025

2007: 12008: 12010: 12011: 42012: 42013: 52014: 32015: 42016: 32017: 12018: 12020: 42021: 22023: 52024: 12025: 12026 (partial year): 1
2007high 5 (2013) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CHL

267in 2023

2011: 108 days median2012: 65 days median2013: 152 days median2014: 68 days median2015: 155 days median2016: 306 days median2020: 100 days median2023: 267 days median
2007high 306 (2016) · low 65 (2012)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · CHL

13so far in 2026, the most since 2007

2007: 62008: 52009: 62010: 72011: 12012: 92013: 12014: 12015: 32016: 12017: 12018: 32020: 22023: 42024: 92026 (partial year): 13
2007high 13 (2026) · low 0 (2019)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · CHL

210in 2025

2007: 162008: 402009: 742010: 202011: 502012: 642013: 622014: 932015: 552016: 1182017: 2062018: 1742019: 1412020: 1172021: 1472022: 1382023: 1772024: 1962025: 210
2007high 210 (2025) · low 16 (2007)2025

MAUDE reports naming product code CHL, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—616
20081—540
20090—674
20101—720
20114108150
2012465964
20135152162
2014368193
20154155355
201633061118
20171—1206
20181—3174
20190—0141
202041002117
20212—0147
20220—0138
202352674177
20241—9196
20251—0210
20261—13—
Cite this page

510(k) Report. “K935069: IL1430 Bgelectrolyte Analyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K935069

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026